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GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST

K935177 Class I Traditional
Decision Date
1993-12-16
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K935177
Product Code JQB
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1360
Decision Date 1993-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GAMMA-GLUTAMYL TRANSFERASE (GGT) TEST received FDA 510(k) clearance under submission number K935177, sponsored by Em Diagnostic Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1993-12-16.

Classification & Regulation

This clearance is catalogued under FDA product code JQB and 21 CFR 862.1360, within the Clinical Chemistry review panel as a Class I device.